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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
PI3K/Akt/mTOR
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TGF-beta/Smad
Ubiquitin
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Cas Index 1
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Cas Index 1
1093403-33-8 | SRT2104
(Catalog# : 16071014)
SRT2104, also known as GSK2245840, is a novel, first-in-class, highly selective small
1359164-11-6 | SR-2211
(Catalog# : 16071002)
SR-2211
1022150-57-7 | SGX-523
(Catalog# : 16070912)
SGX523 is a novel, ATP-competitive kinase inhibitor remarkable for its exquisite sele
160162-42-5 | SR 11302
(Catalog# : 16070908)
SR 11302
1239875-86-5 | SGI 7079
(Catalog# : 16070902)
SGI 7079
125941-87-9 | SCH23390
(Catalog# : 16070103)
SCH23390
130495-35-1 | SKF-96365 HCl
(Catalog# : 16062905)
SKF-96365 is a selective TRPC channel blocker. SKF-96365 activates cytoprotective aut
163169-15-1 | (S)-4-tert-Butyl-2-[(SP)-2-(diphenylphosphino)ferrocenyl]-2-oxazoline
(Catalog# : 16062106)
(S)-4-tert-Butyl-2-[(SP)-2-(diphenylphosphino)ferrocenyl]-2-oxazoline
160098-96-4 | SCH-58261
(Catalog# : 16060802)
SCH-58261 is a potent and selective adenosine A(2A) receptor antagonist. SCH-58261 is
151823-14-2 | Sapacitabine
(Catalog# : 031703)
Sapacitabine is an orally bioavailable pyrimidine analogue prodrug with potential ant
149845-06-7 | Saquinavir Mesylate
(Catalog# : 031701)
Saquinavir mesylate is an HIV protease inhibitor which acts as an analog of an HIV pr
1379686-30-2 | SR9009
(Catalog# : 030908)
Coming soon!
1206194-91-3 | SCHEMBL2274423
(Catalog# : 011917)
Coming soon!
174575-17-8 | SDZ 220-581
(Catalog# : 011901)
SDZ 220-581 is a potent, competitive antagonist at the NMDA glutamate receptor subtyp
181632-25-7 | SB 242084
(Catalog# : 010427)
SB 242084 is a 5-HT2C receptor antagonist(pKi=9.0) that displays 158- and 100-fold se
1025065-69-3 | SGI-1776
(Catalog# : 122945)
SGI-1776 is a novel ATP competitive inhibitor of Pim1 with IC50 of 7 nM; 50- and 10-f
122547-72-2 | Soraphen A
(Catalog# : 122922)
Coming soon!
1561178-17-3 | SGC0946
(Catalog# : 122504)
SGC0946 is a highly potent and selective DOT1L methyltransferase inhibitor with IC50
128427-05-4 | (S)-2-Ethylpiperazine dihydrochloride
(Catalog# : 122503)
Coming soon!
1221411-72-8 | SP-420
(Catalog# : 122304)
SP-420 is an orally active small molecule that selectively binds iron and removes it
1123837-84-2 | Sitravatinib (MGCD516)
(Catalog# : 178906)
Sitravatinib, also known as MGCD516 or MG516, is a novel small molecule inhibitor tar
1262888-28-7 | Spautin-1
(Catalog# : 102622)
Spautin-1 is a novel autophagy inhibitor, IM inhibited the growth of K562 cells with
1234708-04-3 | SAR191801
(Catalog# : 101917)
Coming soon!
1516895-53-6 | SEP-0372814
(Catalog# : 101913)
Coming soon!
1423715-09-6 | SP-2509
(Catalog# : 101909)
SP-2509 is a novel histone demethylase LSD1 inhibitor, which showed high actitivity o
193551-21-2 | SB239063
(Catalog# : 101908)
SB 239063 is a potent p38MAPK inhibitor, which had an IC(50) of 44 nM for inhibition
1174161-69-3 | SCR-1481B1
(Catalog# : 101901)
SCR-1481B1 is a potent and selective MET inhibitor. SCR-1481B1 inhibited MET kinase w
1448428-04-3 | Selonsertib(GS-4997)
(Catalog# : 100503)
Selonsertib is a apoptosis signal-regulating kinase inhibitor (ASK1). Selonsertib may
1421249-72-0 | (1S,3r,5R)-8-(5,6,7,8-tetrahydro-6-(5-isopropyl-2-methylphenyl)-2-(3,5-dimethyl-1H-indazol-4-yl)
(Catalog# : 91813)
Coming soon!
135383-60-7 | (S)-2-phenyl-1-(thiazol-2-yl)ethanaMine hydrochloride
(Catalog# : 91811)
Coming soon!
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Products Catalog
Signaling Pathway
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Src
----
ALK
----
Syk
----
HIF
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
----
Eukaryotic Initiation Factor (eIF)
----
NEKs
-- Cytoskeleton
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
----
Gap Junction Protein
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
----
Methionine Adenosyltransferase (MAT)
-- GPCR & G Protein
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
Endothelin Receptor
----
SGLT
----
OX Receptor
----
CaSR
----
CXCR
----
Vasopressin Receptor
----
Glucagon Receptor
----
Prostaglandin Receptor
----
5-HT Receptor
----
Adrenergic Receptor
----
Cannabinoid Receptor
----
Sphingosine 1 Phosphate Receptor
----
PKA
----
Adenosine Receptor
----
GnRH
----
LPL Receptor
----
Ras
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
----
Bradykinin Receptor
----
GLP Receptor
----
SSTR
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Membrane Transporter/Ion Channel
----
BCRP
----
CFTR
----
EAAT2
----
GABA Receptor
----
HCN Channel
----
Monoamine Transporter
----
Na+/Ca2+ Exchanger
----
Na+/K+ ATPase
----
nAChR
----
Calcium Channel
----
Chloride Channel
----
CRAC Channel
----
GlyT1
----
iGluR
----
P2X Receptor
----
P-glycoprotein
----
Amino acid transporter
----
Monocarboxylate Transporter
----
Potassium Channel
----
Proton Pump
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
----
Hemoglobin
-- Neuronal Signaling
----
COX
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
GABA Receptor
----
OX Receptor
----
Amyloid-β
----
5-HT Receptor
----
γ-secretase
----
Adrenergic Receptor
----
NMDA Receptor
----
GlyT1
----
Beta-secretase
----
Sigma Receptor
----
mAChR
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
----
Melanocortin Receptor
----
Glucosylceramide Synthase (GCS)
----
CGRP-Receptor
----
TRP-Channel
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
----
Keap1-Nrf2
-- Protein Tyrosine Kinase
----
VEGFR
----
EGFR
----
PDGFR
----
IGF-1R
----
FLT3
----
FGFR
----
c-Kit
----
Src
----
ALK
----
Ephrin receptor
----
BTK
----
Trk receptor
----
c-Met/HGFR
----
Syk (Spleen tyrosine kinase)
----
TAM Receptor
----
ULK1
----
CSF-1R
----
TYK2
----
ROS Kinase
----
Bcr-Abl
----
FAK
----
RET
----
Phosphoglycerate Kinase (PGK)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- TGF-beta/Smad
----
PKC
----
ROCK
----
TGF-beta/Smad
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
----
DUB
-- Vitamin D Related
----
VD/VDR
-- PROTAC
----
Molecular Glues
----
PROTACs
--
Antibody-drug Conjugate/ADC Related
--
Microbiology
-- Others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
----
Newest added products
-- Nuclear Receptor
----
Androgen Receptor(AR)
Inhibitors & Agonists
Intermediates
Building Blocks
--
Aldehydes
--
Amines
--
Amino Acids
--
Anilines
--
Boronic Acids
--
Bromides
--
Carboxes
--
Catalysts
--
Chiral Compounds
--
Deuterated
--
Fluorides
--
Imidazoles
--
Indoles and Oxindoles
--
Iodos
--
Nitro Compounds
--
Oxazoles
--
Peg Linkers
--
Phenols
--
Piperidines
--
Pyridines
--
Pyrimidines
--
Quinolines
--
Sulfonamides
--
Thiazoles
--
Trifluoroborates
--
Other Azoles
--
Other Heterocycles
--
Other Building Blocks
--
On Sale
New Products
Natural Compounds
Latest Products
1429882-07-4 | MRX-2843
(Catalog# : 26A087)
MRX-2843 is an orally bioavailable inhibitor of two receptor tyrosine kinases (RTKs),
1637394-01-4 | GDC-0134
(Catalog# : 20432)
GDC-0134 is a MAP3K12 (DLK) Inhibitor.
2128698-24-6 | BI-847325
(Catalog# : 25046)
BI-847325 is a novel, ATP-competitive, orally available inhibitor of Aurora kinases a
3137699-54-5 | GDD-261
(Catalog# : 26A084)
GDD-261 is an orally active, allosteric inhibitor of phosphoglycerate dehydrogenase (
2669009-92-9 | Atebimetinib
(Catalog# : 25148)
Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1
3062177-59-4 | BH-30643
(Catalog# : 26A047)
BH-30643 is a novel, orally available, non-covalent, macrocyclic, mutant selective OM
2490431-16-6 | ERAS-801 ( JGK-068S )
(Catalog# : 20635)
ERAS-801 ( JGK-068S ) is a potent EGFR inhibitor.
877176-23-3 | Aderamastat ( Synonyms: FP-025 )
(Catalog# : 26A086)
Aderamastat (FP-025) is an oral, selective, non-hydroxamate-based, non-competitive in
1857296-22-0 | 5-Formyl-4-methyl-1H-indole-2-carbonitrile
(Catalog# : 25095)
2923986-48-3 | MAT2A inhibitor-[Compound 1]
(Catalog# : 26A083)
Compound 1 is a new MAT2A inhibitor.